Butyl Acrylate → butylacrylate methoxyethylacrylate N,N-dimethylacrylamide

HRID 2051463

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HRID 2051463 반응식
[CH2:1]([O:5][C:6](=[O:9])[CH:7]=[CH2:8])[CH2:2][CH2:3][CH3:4].[CH3:10][O:11][CH2:12][CH2:13][O:14][C:15](=[O:18])[CH:16]=[CH2:17].[CH3:19][N:20]([CH3:25])[C:21](=[O:24])[CH:22]=[CH2:23]>>[CH2:1]([O:5][C:6](=[O:9])[CH:7]=[CH2:8])[CH2:2][CH2:3][CH3:4].[CH3:10][O:11][CH2:12][CH2:13][O:14][C:15](=[O:18])[CH:16]=[CH2:17].[CH3:19][N:20]([CH3:25])[C:21](=[O:24])[CH:22]=[CH2:23]

참가 물질

4

실험 절차

A 25:25:50 (weight percent) butylacrylate/methoxyethylacrylate/N,N-dimethylacrylamide copolymer is prepared as follows. Butylacrylate, methoxyethylacrylate, and N,N-dimethylacrylamide are weighed out (relative weight ratios of 25:25:50) and added to a three neck flask fitted with an argon sparge, mechanical stirrer and condenser. Toluene is then added to the flask to get a final monomer concentration of 20.0 weight percent. The reaction flask is placed in a 60° C. water bath and the reaction mixture is sparged with argon for two hours while stirring. After two hours, azobisisobutyronitrile ("AIBN") is added to the reaction flask in an amount sufficient to get a final initiator concentration of 0.05 weight percent. The reaction is then stirred for two hours, after which time the reaction flask is removed from the water bath and the reaction mixture is poured into a container of hexane to precipitate the copolymer. The copolymer is then removed from the hexane, placed in a polyethylene tray, and dried in a vacuum oven at 30° C. In order to remove any residual monomer, the dried copolymer is dissolved in toluene, reprecipitated in hexane, and then dried again in a vacuum oven. The glass transition temperature of this copolymer is calculated to be approximately 21° C.

후처리

  1. additionadded to a three neck flask
  2. customfitted with an argon
  3. customsparge
  4. additionToluene is then added to the flask

출처 및 근거

ORD 기록
ord-56544a28fe224e18a875b20a44cdb2d8
출처 데이터셋
uspto-grants-1991_05
특허 번호
US05019377

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